Evidence that the respiratory syncytial virus polymerase complex associates with lipid rafts in virus-infected cells: a proteomic analysis
Creators
- 1. MRC Virology Unit, Institute of Virology, Glasgow G11 5JR (United Kingdom)
- 2. Sir Henry Wellcome Functional Genomics Facility, University of Glasgow, Glasgow, G12 8QQ (United Kingdom)
Description
The interaction between the respiratory syncytial virus (RSV) polymerase complex and lipid rafts was examined in HEp2 cells. Lipid-raft membranes were prepared from virus-infected cells and their protein content was analysed by Western blotting and mass spectrometry. This analysis revealed the presence of the N, P, L, M2-1 and M proteins. However, these proteins appeared to differ from one another in their association with these structures, with the M2-1 protein showing a greater partitioning into raft membranes compared to that of the N, P or M proteins. Determination of the polymerase activity profile of the gradient fractions revealed that 95% of the detectable viral enzyme activity was associated with lipid-raft membranes. Furthermore, analysis of virus-infected cells by confocal microscopy suggested an association between these proteins and the raft-lipid, GM1. Together, these results provide evidence that the RSV polymerase complex is able to associate with lipid rafts in virus-infected cells
Additional details
Identifiers
- DOI
- 10.1016/j.virol.2004.09.034;
- PII
- S0042-6822(04)00648-8;
Publishing Information
- Journal Title
- Virology
- Journal Volume
- 330
- Journal Issue
- 1
- Journal Page Range
- p. 147-157
- ISSN
- 0042-6822
- CODEN
- VIRLAX
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36080514
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ENZYME ACTIVITY; INTERACTIONS; LIPIDS; MASS SPECTROSCOPY; MEMBRANES; MICROSCOPY; PROTEINS; VIRUSES
- Descriptors DEC
- MICROORGANISMS; ORGANIC COMPOUNDS; PARASITES; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.